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通过荧光寿命成像显微镜对卵丘细胞、卵子和胚胎进行无创代谢轮廓分析:小型综述。

Noninvasive metabolic profiling of cumulus cells, oocytes, and embryos via fluorescence lifetime imaging microscopy: a mini-review.

机构信息

Molecular and Cellular Biology and School of Engineering and Applied Sciences, Harvard University, Cambridge, MA, USA.

Boston IVF-The Eugin Group, Waltham, MA, USA.

出版信息

Hum Reprod. 2023 May 2;38(5):799-810. doi: 10.1093/humrep/dead063.

Abstract

A major challenge in ART is to select high-quality oocytes and embryos. The metabolism of oocytes and embryos has long been linked to their viability, suggesting the potential utility of metabolic measurements to aid in selection. Here, we review recent work on noninvasive metabolic imaging of cumulus cells, oocytes, and embryos. We focus our discussion on fluorescence lifetime imaging microscopy (FLIM) of the autofluorescent coenzymes NAD(P)H and flavine adenine dinucleotide (FAD+), which play central roles in many metabolic pathways. FLIM measurements provide quantitative information on NAD(P)H and FAD+ concentrations and engagement with enzymes, leading to a robust means of characterizing the metabolic state of cells. We argue that FLIM is a promising approach to aid in oocyte and embryo selection.

摘要

ART 面临的主要挑战之一是选择高质量的卵母细胞和胚胎。卵母细胞和胚胎的代谢与其活力长期以来一直相关,这表明代谢测量在辅助选择方面具有潜在的应用价值。在这里,我们回顾了关于卵丘细胞、卵母细胞和胚胎的非侵入性代谢成像的最新研究。我们的讨论重点是荧光寿命成像显微镜(FLIM)对辅酶 NAD(P)H 和黄素腺嘌呤二核苷酸(FAD+)的荧光寿命成像,它们在许多代谢途径中发挥着核心作用。FLIM 测量提供了有关 NAD(P)H 和 FAD+浓度以及与酶相互作用的定量信息,从而为细胞代谢状态的特征提供了一种稳健的方法。我们认为,FLIM 是一种很有前途的辅助卵母细胞和胚胎选择的方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2b9a/10152178/1db2ec12a751/dead063f4.jpg

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